FDA 510(k) Application Details - K182418

Device Classification Name	Appliance, Fixation, Spinal Intervertebral Body   More FDA Info for this Device
510(K) Number	K182418
Device Name	Appliance, Fixation, Spinal Intervertebral Body
Applicant	Atlas Spine, Inc. 1555 Jupiter Park Drive, Suite 1 Jupiter, FL 33458 US Other 510(k) Applications for this Company
Contact	Thomas Smith Other 510(k) Applications for this Contact
Regulation Number	888.3060   More FDA Info for this Regulation Number
Classification Product Code	KWQ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/05/2018
Decision Date	11/29/2018
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review